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T Voit

Showing results (51-60 of 143) with videos related to

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FEBS Letters|June 8, 2001
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 geneJ Klepper, I Monden, E Guertsen, et al.
Annals of Neurology|May 19, 2001
Hypoglycorrhachia: a simple clue, simply missedM A Willemsen, A Verrips, M M Verbeek, et al.
Clinical Neuropathology|November 1, 1987
Neonatal myotonic dystrophy in a premature infant: clinical and morphological findingsE Neuen-Jacob, T Voit, J Turski, et al.
The American Journal of Pathology|November 1, 1991
Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodiesT Voit, K Haas, J O Léger, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal musclesF Pons, L V Nicholson, A Robert, et al.
Neurology|July 23, 1998
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild casesR D Cohn, R Herrmann, L Sorokin, et al.
Neurology|February 12, 2004
Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2IC Dohna-Schwake, R Ragette, U Mellies, et al.
The New England Journal of Medicine|September 14, 1995
Serum antibodies to the deleted dystrophin sequence after cardiac transplantation in a patient with Becker's muscular dystrophyR E Bittner, S Shorny, B Streubel, et al.
The European Respiratory Journal|October 30, 2003
Long-term noninvasive ventilation in children and adolescents with neuromuscular disordersU Mellies, R Ragette, C Dohna Schwake, et al.
Neurology|April 27, 2005
Respiratory failure in Pompe disease: treatment with noninvasive ventilationU Mellies, F Stehling, C Dohna-Schwake, et al.
Pageof 15

Showing results (51-60 of 143) with videos related to

Sort By:
Pageof 15
FEBS Letters|June 8, 2001
Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 geneJ Klepper, I Monden, E Guertsen, et al.
Annals of Neurology|May 19, 2001
Hypoglycorrhachia: a simple clue, simply missedM A Willemsen, A Verrips, M M Verbeek, et al.
Clinical Neuropathology|November 1, 1987
Neonatal myotonic dystrophy in a premature infant: clinical and morphological findingsE Neuen-Jacob, T Voit, J Turski, et al.
The American Journal of Pathology|November 1, 1991
Xp21 dystrophin and 6q dystrophin-related protein. Comparative immunolocalization using multiple antibodiesT Voit, K Haas, J O Léger, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Dystrophin and dystrophin-related protein (utrophin) distribution in normal and dystrophin-deficient skeletal musclesF Pons, L V Nicholson, A Robert, et al.
Neurology|July 23, 1998
Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild casesR D Cohn, R Herrmann, L Sorokin, et al.
Neurology|February 12, 2004
Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2IC Dohna-Schwake, R Ragette, U Mellies, et al.
The New England Journal of Medicine|September 14, 1995
Serum antibodies to the deleted dystrophin sequence after cardiac transplantation in a patient with Becker's muscular dystrophyR E Bittner, S Shorny, B Streubel, et al.
The European Respiratory Journal|October 30, 2003
Long-term noninvasive ventilation in children and adolescents with neuromuscular disordersU Mellies, R Ragette, C Dohna Schwake, et al.
Neurology|April 27, 2005
Respiratory failure in Pompe disease: treatment with noninvasive ventilationU Mellies, F Stehling, C Dohna-Schwake, et al.
Pageof 15